Canonical Allele Identifier: CA467653289
Gene: COL5A1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.137642647A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.134750801A>C , CM000671.2:g.134750801A>C GRCh38
NC_000009.11:g.137642647A>C , CM000671.1:g.137642647A>C GRCh37
NC_000009.10:g.136782468A>C NCBI36
NG_008030.1:g.113996A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000371820.4:c.1581A>C ENSP00000360885.4:p.Gly527=
ENST00000371817.8:c.1581A>C MANE Select ENSP00000360882.3:p.Gly527=
ENST00000371817.7:c.1581A>C ENSP00000360882.3:p.Gly527=
ENST00000618395.4:c.1581A>C ENSP00000481360.1:p.Gly527=
NM_000093.4:c.1581A>C NP_000084.3:p.Gly527=
NM_001278074.1:c.1581A>C NP_001265003.1:p.Gly527=
XR_929712.1:n.1983A>C
XR_929713.1:n.1983A>C
XM_017014266.2:c.1581A>C XP_016869755.1:p.Gly527=
XR_001746183.1:n.1979A>C
NM_000093.5:c.1581A>C MANE Select NP_000084.3:p.Gly527=